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Journal Abstract Search
352 related items for PubMed ID: 18411802
1. [Characterization of a large deletion that leads to congenital factor XIII deficiency]. Otaki M, Inaba H, Shinozawa K, Fujita S, Amano K, Fukutake K. Rinsho Byori; 2008 Mar; 56(3):187-94. PubMed ID: 18411802 [Abstract] [Full Text] [Related]
2. Deficiency of coagulation factor XIII A subunit caused by the dinucleotide deletion at the 5' end of exon III. Kamura T, Okamura T, Murakawa M, Tsuda H, Teshima T, Shibuya T, Harada M, Niho Y. J Clin Invest; 1992 Aug; 90(2):315-9. PubMed ID: 1644910 [Abstract] [Full Text] [Related]
3. Gene defects in congenital factor XIII deficiency. Mikkola H, Palotie A. Semin Thromb Hemost; 1996 Aug; 22(5):393-8. PubMed ID: 8989822 [Abstract] [Full Text] [Related]
5. Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiency. Izumi T, Nagaoka U, Saito T, Takamatsu J, Saito H, Ichinose A. Thromb Haemost; 1998 Mar; 79(3):479-85. PubMed ID: 9531026 [Abstract] [Full Text] [Related]
7. Congenital factor XIII deficiency caused by two mutations in eight Tunisian families: molecular confirmation of a founder effect. Louhichi N, Medhaffar M, Hadjsalem I, Mkaouar-Rebai E, Fendri-Kriaa N, Kanoun H, Yaïch F, Souissi T, Elloumi M, Fakhfakh F. Ann Hematol; 2010 May; 89(5):499-504. PubMed ID: 19937244 [Abstract] [Full Text] [Related]
8. [Identification of two novel mutation in two Chinese hereditary coagulation factor XIII deficiency families]. Duan B, Wang H, Chu H, Wang X, Qu B, Li D, Wang H, Yin J, Kang W, Wang Z. Zhonghua Xue Ye Xue Za Zhi; 2002 Mar; 23(3):117-20. PubMed ID: 12015062 [Abstract] [Full Text] [Related]